Canonical Allele Identifier: CA890035977

Gene: LINC02819

Linked Data

• dbSNP Id: rs766549821
• gnomAD v3: 1-159484164-C-A
• gnomAD v4: 1-159484164-C-A
• MyVariant Identifiers: chr1:g.159453954C>A (hg19) ; chr1:g.159484164C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159484164C>A , CM000663.2:g.159484164C>A	GRCh38
NC_000001.10:g.159453954C>A , CM000663.1:g.159453954C>A	GRCh37
NC_000001.9:g.157720578C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_922189.1:n.678+1180C>A
XR_922189.3:n.690+1180C>A